High recovery process for purification of multicomponent gases
The process of the present invention provides high recovery and low capital cost giving it an economic advantage over previously known purification processes. The present process has particular applicability to the purification of synthesis gases comprising at least hydrogen (H 2 ), carbon monoxide (CO), methane (CH 4 ), CO 2 , and H 2 O to obtain a gas stream including at least H 2 , CO, and CH 4 , that is substantially free of H 2 O and CO 2 . The process also has applicability to the purification of natural gases inclusive of at least CH 4 , N 2 , CO 2 , and H 2 O to produce a gas stream including at least CH 4 and N 2 , but which is substantially free of H 2 O and CO 2 .
1 . A cyclic pressure swing adsorption (PSA) process for the substantial removal of H 2 O and CO 2 comprising: contacting a multicomponent feed gas at elevated pressure with an adsorbent bed wherein the adsorbent bed comprises a layer of activated alumina, a layer of silica gel, and a layer of alkali-promoted alumina to obtain a multicomponent product gas substantially free of H 2 O and CO 2 with high recovery of the product gas components, the process wherein a plurality of adsorbent beds in a PSA system are subjected to a series of process steps which include an adsorption step, three or more pressure equalization steps at decreasing pressure, a blowdown step, a purge step in which a purge gas comprises a portion of the product gas or a gas originating externally from the process that is substantially free of H 2 O and CO 2 and comprises at least one of the major components of the product gas, three or more pressure equalization steps at increasing pressure, and a final repressurization step, wherein each of the adsorbent beds contains at least one adsorbent layer for the substantial removal of CO 2 characterized by:
i.a CO 2 loading capacity of greater than or equal to 0.1 mol CO 2 per kg of adsorbent at a CO 2 partial pressure of 1000 Pa at 300 K, and
ii.a differential capacity of the product gas components of less than or equal to 0.1 mol per kg of adsorbent, where the differential capacity is defined as the difference between the loading capacity at partial pressures of 100,000 Pa and 10,000 Pa at 300 K;
and wherein the high recovery of the product gas components is an amount greater than or equal to 80%, where recovery, X i herein defined as the flow rate of each component in the product gas relative to the flow rate of each component in the feed gas and is expressed algebraically as:
X
i
[
%
]
=
F
Product
·
y
Product
i
F
Feed
·
y
Feed
i
·
100
%
where:
i: gas component index (H 2 , CO, CH 4 )
F product : flow rate of the product gas
F Feed : flow rate of the feed gas
y
Product
i
:
concentration of component i in the product gas
y
F
e
e
d
i
:
concentration of component i in the feed gas.
2 . The cyclic PSA process of claim 1 , wherein the H 2 O concentration in the multicomponent product gas is less than or equal to 10 ppb, and CO 2 is removed to below 100 ppb.
3 . The cyclic PSA process of claim 1 , wherein the adsorbent bed contains at least one layer of activated alumina or alkali-promoted alumina.
4 . The cyclic PSA process of claim 1 , wherein a number of successive countercurrent depressurization steps is greater than or equal to 4.
5 . The cyclic PSA process of claim 1 , wherein the number of successive countercurrent depressurization steps is greater than or equal to 5.
6 . The cyclic PSA process of claim 1 , wherein a number of adsorbent beds simultaneously processing feed gas is 2.
7 . The cyclic PSA process of claim 1 , wherein a number of adsorbent beds simultaneously processing feed gas is 3.
8 . The cyclic PSA process of claim 1 , wherein the feed gas is a synthesis gas comprising at least H 2 , CO, CH 4 , CO 2 , and H 2 O with a high recovery of H 2 and CO.
9 . The cyclic PSA process of claim 1 , wherein the feed gas is a natural gas comprising at least CH 4 , N 2 , CO 2 , and H 2 O with a high recovery of CH 4 and N 2 .
10 . The cyclic PSA process of claim 1 , wherein the purge gas is provided from a cryogenic separation unit or a H 2 PSA or a membrane unit.
11 . The cyclic PSA process of claim 8 , wherein the synthesis gas is produced via steam methane reforming, autothermal reforming, or partial oxidation.
12 . The cyclic PSA process of claim 7 , wherein the purge gas is a tail gas from a H 2 PSA or a membrane unit.
13 . The cyclic PSA process of claim 7 , wherein the purge gas is a flash gas or crude H 2 gas from a cryogenic separation unit.